Disease #00300 (PAPA1;PAPB (polydactyly, postaxial, type A1 (PAPA-1, type B included (PAPB))), OMIM:174200)
| Official abbreviation |
PAPA1;PAPB |
| Name |
polydactyly, postaxial, type A1 (PAPA-1, type B included (PAPB)) |
| OMIM ID |
174200 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
GLI3 |
| Associated tissues |
- |
| Disease features |
autosomal dominant |
| Remarks |
- |
| Date created |
2014-01-19 11:19:19 +01:00 (CET) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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